Junior Clinical Research Coordinator

CARE; Quincy (MA); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Paid Time Off (PTO)

Health insurance

401(k) retirement plan

Health Savings Account (HSA)

Short-Term Disability

Job summary

Care Access is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects in compliance with GCP and regulatory standards. This onsite role requires attention to protocol timelines and accurate data entry while maintaining patient privacy and safety.

Responsibilities include coordinating visits, obtaining informed consent, reviewing lab results, and communicating with investigators and sponsor representatives.

Qualifications

• Bachelor’s degree preferred or equivalent education, training, and experience.
• Minimum 1 year of Clinical Research Coordinator experience.
• Recent phlebotomy experience required.

Responsibilities

• Prescreen study candidates and obtain informed consent per SOP.
• Complete visit procedures in accordance with protocol.
• Review laboratory results and ECGs for completeness and alert values.
• Identify adverse events and promptly notify Principal Investigator and Sponsor.
• Maintain regulatory documentation and data entry in real time.

Skills

Communication skills

Regulatory knowledge

GCP/GCP knowledge

Teamwork

Time management

Education

Bachelor’s degree preferred

Tools

Clinical trials database

IVR systems

Electronic data capture

MS Word

Excel

Job description

Care Access is seeking a Clinical Research Coordinator to screen, enroll, and monitor study subjects in compliance with GCP and regulatory standards. This onsite role requires attention to protocol timelines and accurate data entry while maintaining patient privacy and safety.

Responsibilities include coordinating visits, obtaining informed consent, reviewing lab results, and communicating with investigators and sponsor representatives.